NDC 69367-382 – Metformin Hydrochloride
Metformin Hydrochloride 850 mg/1 · Tablet, Coated · Oral
Product NDC69367-382
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205096
- Marketed since
- March 4, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 850 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 69367-382-01 | 100 TABLET, COATED in 1 BOTTLE (69367-382-01) | Mar 4, 2024 |
| 69367-382-05 | 500 TABLET, COATED in 1 BOTTLE (69367-382-05) | Mar 4, 2024 |
| 69367-382-10 | 1000 TABLET, COATED in 1 BOTTLE (69367-382-10) | Mar 4, 2024 |
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